hypergonadotropic hypogonadism-cataract syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0009417


This syndrome is characterized by the association of hypergonadotropic hypogonadism and cataracts with onset during adolescence. It has been described in three brothers from a consanguineous family. [ Orphanet:2410 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:E29.1 (Orphanet:2410)
  • Orphanet:2410 (OMIM:240950)
  • SCTID:721233005 (MONDO:equivalentTo)
  • UMLS:C1855859 (Orphanet:2410)
  • OMIM:240950 (Orphanet:2410)
  • MESH:C543092 (MONDO:equivalentTo)
  • GARD:0000298 (Orphanet-shared)
Subsets

ordo_malformation_syndrome

definition

This syndrome is characterized by the association of hypergonadotropic hypogonadism and cataracts with onset during adolescence. It has been described in three brothers from a consanguineous family.

exactMatch

http://linkedlifedata.com/resource/umls/id/C1855859

http://identifiers.org/omim/240950

http://identifiers.org/mesh/C543092

http://identifiers.org/snomedct/721233005

http://www.orpha.net/ORDO/Orphanet_2410

has exact synonym

Lubinsky syndrome

has related synonym

cataracts and testicular failure

hypogonadism-cataract syndrome

hypogonadism cataract syndrome

id

MONDO:0009417